All Day Relief (naproxen sodium) NDC 56062-748

Product information

Brand name (proprietary)

All Day Relief

Generic name (nonproprietary)

naproxen sodium

Active ingredients

Naproxen sodium — 220 mg/1

Dosage form

Capsule, Liquid filled

Route

Oral

Labeler

Publix Supermarkets, Inc.

Product type

Over-the-counter drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 208363

Marketing start

Jun 30, 2019

Listing expires

Dec 31, 2026

Other FDA classes

Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)

Identifiers

Product ID 56062-748_581830ee-5c9a-40aa-8bf7-c02dcda51e0fSPL ID 581830ee-5c9a-40aa-8bf7-c02dcda51e0fSPL set ID 4db86c5b-62bb-4638-9f1e-98dc2680d6ccRxCUI 1112231UNII 9TN87S3A3C

Pharmacologic class

Nonsteroidal Anti-inflammatory Drug

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N456062074840 followed by a unit qualifier and the quantity Copy

Package 56062-0748-40. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Other NDCs under ANDA 208363

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.